RoyceDerm Anti fungal RELIEF cream

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: RoyceDerm Anti fungal RELIEF cream
Generic name: SALICYLIC ACID 2%
Manufacturer: RoyceDerm LLC
Product type: HUMAN OTC DRUG
SPL set ID: 47ec6277-e40f-af82-e063-6294a90ac8c1
SPL ID: 47ec6277-e410-af82-e063-6294a90ac8c1
Version: 1
Effective date: 2026-01-08
Source export date: 2026-11-06
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/97001096994db9ca8cee114e6c3bb5298d3c573158ffc1ab8692d82e76a3eb40/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 06:56:42

Harmonized routes table
Harmonized routes
TRANSDERMAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M005	openfda.application_number
brand name		RoyceDerm Anti fungal RELIEF cream	openfda.brand_name
generic name		SALICYLIC ACID 2%	openfda.generic_name
manufacturer name		RoyceDerm LLC	openfda.manufacturer_name
ndc	package	85424-013-01	openfda.package_ndc
ndc	product	85424-013	openfda.product_ndc
ndc11	package	85424001301	derived:openfda.package_ndc
spl id		47ec6277-e410-af82-e063-6294a90ac8c1	id
spl set id		47ec6277-e40f-af82-e063-6294a90ac8c1	set_id
unii		FCU6WET6AA	openfda.unii
unii		O414PZ4LPZ	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

FOR EXTERNAL USE ONLY if you are allergic to ingredients in this product. avoid contact with eyes. If contact occurs, rinse the eyes thoroughly with water. condition worsens or does not improve after regular use as directed. If swalloWed,get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.